-
1
-
-
34250824768
-
Catalytic Carbophilic Activation: Catalysis by Platinum and Gold π Acids
-
- 3449
-
Fürstner, A.; Davies, P. W. Catalytic Carbophilic Activation: Catalysis by Platinum and Gold π Acids Angew. Chem., Int. Ed. 2007, 46, 3410-3449
-
(2007)
Angew. Chem., Int. Ed.
, vol.46
, pp. 3410
-
-
Fürstner, A.1
Davies, P.W.2
-
2
-
-
35348824909
-
From σ- to π-Electrophilic Lewis Acids. Application to Selective Organic Transformations
-
- 7831
-
Yamamoto, Y. From σ- to π-Electrophilic Lewis Acids. Application to Selective Organic Transformations J. Org. Chem. 2007, 72, 7817-7831
-
(2007)
J. Org. Chem.
, vol.72
, pp. 7817
-
-
Yamamoto, Y.1
-
3
-
-
33947578482
-
Relativistic Effects in Homogeneous Gold Catalysis
-
- 403
-
Gorin, D. J.; Toste, F. D. Relativistic Effects in Homogeneous Gold Catalysis Nature 2007, 446, 395-403
-
(2007)
Nature
, vol.446
, pp. 395
-
-
Gorin, D.J.1
Toste, F.D.2
-
4
-
-
33846207883
-
Molecular Diversity through Gold Catalysis with Alkynes
-
- 346
-
Jiménez-Núnez, E.; Echavarren, A. M. Molecular Diversity through Gold Catalysis with Alkynes Chem. Commun. 2007, 333-346
-
(2007)
Chem. Commun.
, pp. 333
-
-
Jiménez-Núnez, E.1
Echavarren, A.M.2
-
6
-
-
70350496890
-
Gold and Platinum Catalysis-A Convenient Tool for Generating Molecular Complexity
-
- 3221
-
Fürstner, A. Gold and Platinum Catalysis-A Convenient Tool for Generating Molecular Complexity Chem. Soc. Rev. 2009, 38, 3208-3221
-
(2009)
Chem. Soc. Rev.
, vol.38
, pp. 3208
-
-
Fürstner, A.1
-
7
-
-
0032569211
-
Platinum- and Acid-Catalyzed Enyne Metathesis Reactions: Mechanistic Studies and Applications to the Syntheses of Streptorubin B and Metacycloprodigiosin
-
- 8314
-
Fürstner, A.; Szillat, H.; Gabor, B.; Mynott, R. Platinum- and Acid-Catalyzed Enyne Metathesis Reactions: Mechanistic Studies and Applications to the Syntheses of Streptorubin B and Metacycloprodigiosin J. Am. Chem. Soc. 1998, 120, 8305-8314
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 8305
-
-
Fürstner, A.1
Szillat, H.2
Gabor, B.3
Mynott, R.4
-
8
-
-
0035814401
-
Platinum-Catalyzed Cycloisomerization Reactions of Enynes
-
- 11869
-
Fürstner, A.; Stelzer, F.; Szillat, H. Platinum-Catalyzed Cycloisomerization Reactions of Enynes J. Am. Chem. Soc. 2001, 123, 11863-11869
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 11863
-
-
Fürstner, A.1
Stelzer, F.2
Szillat, H.3
-
9
-
-
84880149095
-
Direct syn Insertion of Alkynes and Allenes into Au-Si Bonds
-
For a pertinent example, see - 7163
-
For a pertinent example, see: Joost, M.; Gualco, P.; Mallet-Ladeira, S.; Amgoune, A.; Bourissou, D. Direct syn Insertion of Alkynes and Allenes into Au-Si Bonds Angew. Chem., Int. Ed. 2013, 52, 7160-7163
-
(2013)
Angew. Chem., Int. Ed.
, vol.52
, pp. 7160
-
-
Joost, M.1
Gualco, P.2
Mallet-Ladeira, S.3
Amgoune, A.4
Bourissou, D.5
-
10
-
-
84861510526
-
Diversity-Oriented Synthesis of Diverse Polycyclic Scaffolds Inspired by the Logic of Sesquiterpene Lactones Biosynthesis
-
For an instructive recent study, see - 5394
-
For an instructive recent study, see: Valot, G.; Garcia, J.; Duplan, V.; Serba, C.; Barluenga, S.; Winssinger, N. Diversity-Oriented Synthesis of Diverse Polycyclic Scaffolds Inspired by the Logic of Sesquiterpene Lactones Biosynthesis Angew. Chem., Int. Ed. 2012, 51, 5391-5394
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 5391
-
-
Valot, G.1
Garcia, J.2
Duplan, V.3
Serba, C.4
Barluenga, S.5
Winssinger, N.6
-
11
-
-
77952337752
-
Gold Catalysis: Recent Developments and Future Trends
-
- 251
-
Nevado, C. Gold Catalysis: Recent Developments and Future Trends Chimia 2010, 64, 247-251
-
(2010)
Chimia
, vol.64
, pp. 247
-
-
Nevado, C.1
-
12
-
-
84857594600
-
Gold Catalysis in Total Synthesis - an Update
-
- 2462
-
Rudolph, M.; Hashmi, A. S. K. Gold Catalysis in Total Synthesis-an Update Chem. Soc. Rev. 2012, 41, 2448-2462
-
(2012)
Chem. Soc. Rev.
, vol.41
, pp. 2448
-
-
Rudolph, M.1
Hashmi, A.S.K.2
-
13
-
-
84865842560
-
Gold in Total Synthesis: Alkynes as Carbonyl Surrogates
-
- 8935
-
Brenzovick, W. E., Jr. Gold in Total Synthesis: Alkynes as Carbonyl Surrogates Angew. Chem., Int. Ed. 2012, 51, 8933-8935
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 8933
-
-
Brenzovick Jr., W.E.1
-
14
-
-
0001525502
-
2-Catalyzed Conversion of 1,6- and 1,7-Enynes to 1-Vinylcycloalkenes. Anomalous Bond Connection in Skeletal Reorganization of Enynes
-
- 903
-
2-Catalyzed Conversion of 1,6- and 1,7-Enynes to 1-Vinylcycloalkenes. Anomalous Bond Connection in Skeletal Reorganization of Enynes Organometallics 1996, 15, 901-903
-
(1996)
Organometallics
, vol.15
, pp. 901
-
-
Chatani, N.1
Furukawa, N.2
Sakurai, H.3
Murai, S.4
-
15
-
-
17744417463
-
Chemistry and Biology of Roseophilin and the Prodigiosin Alkaloids: A Survey of the Last 2500 Years
-
- 3603
-
Fürstner, A. Chemistry and Biology of Roseophilin and the Prodigiosin Alkaloids: A Survey of the Last 2500 Years Angew. Chem., Int. Ed. 2003, 42, 3582-3603
-
(2003)
Angew. Chem., Int. Ed.
, vol.42
, pp. 3582
-
-
Fürstner, A.1
-
16
-
-
69249202400
-
A Bonding Model for Gold(I) Carbene Complexes
-
For a pertinent later discussion of the cation/carbene continuum, see - 486
-
For a pertinent later discussion of the cation/carbene continuum, see: Benitez, D.; Shapiro, N. D.; Tkatchouck, E.; Wang, Y.; Goddard, W. A.; Toste, F. D. A Bonding Model for Gold(I) Carbene Complexes Nat. Chem. 2009, 1, 482-486
-
(2009)
Nat. Chem.
, vol.1
, pp. 482
-
-
Benitez, D.1
Shapiro, N.D.2
Tkatchouck, E.3
Wang, Y.4
Goddard, W.A.5
Toste, F.D.6
-
17
-
-
53049098944
-
On the Nature of the Reactive Intermediates in Gold-Catalyzed Cycloisomerization Reactions
-
The arguably most convincing example is the emulation of the Stork-Eschenmoser paradigm of cationic polycyclization reactions by gold-catalyzed cyclization cascades, see - 5033
-
The arguably most convincing example is the emulation of the Stork-Eschenmoser paradigm of cationic polycyclization reactions by gold-catalyzed cyclization cascades, see: Fürstner, A.; Morency, L. On the Nature of the Reactive Intermediates in Gold-Catalyzed Cycloisomerization Reactions Angew. Chem., Int. Ed. 2008, 47, 5030-5033
-
(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 5030
-
-
Fürstner, A.1
Morency, L.2
-
18
-
-
70349778993
-
Elementary Steps of Gold Catalysis: NMR Spectroscopy Reveals the Highly Cationic Character of a "Gold Carbenoid"
-
- 2513
-
Seidel, G.; Mynott, R.; Fürstner, A. Elementary Steps of Gold Catalysis: NMR Spectroscopy Reveals the Highly Cationic Character of a "Gold Carbenoid" Angew. Chem., Int. Ed. 2009, 48, 2510-2513
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 2510
-
-
Seidel, G.1
Mynott, R.2
Fürstner, A.3
-
19
-
-
84878693560
-
Direct Observation of a Cationic Gold(I)-Bicyclo[3.2.0]hept-1(7)-ene Complex Generated in the Cycloisomerization of a 7-Phenyl-1,6-enyne
-
- 6261
-
Brooner, R. E. M.; Brown, T. J.; Widenhoefer, R. A. Direct Observation of a Cationic Gold(I)-Bicyclo[3.2.0]hept-1(7)-ene Complex Generated in the Cycloisomerization of a 7-Phenyl-1,6-enyne Angew. Chem., Int. Ed. 2013, 52, 6259-6261
-
(2013)
Angew. Chem., Int. Ed.
, vol.52
, pp. 6259
-
-
Brooner, R.E.M.1
Brown, T.J.2
Widenhoefer, R.A.3
-
20
-
-
20444496467
-
Cyclobutenes by Platinum-Catalyzed Cycloisomerization Reactions of Enynes
-
- 8245
-
Fürstner, A.; Davies, P. W.; Gress, T. Cyclobutenes by Platinum-Catalyzed Cycloisomerization Reactions of Enynes J. Am. Chem. Soc. 2005, 127, 8244-8245
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 8244
-
-
Fürstner, A.1
Davies, P.W.2
Gress, T.3
-
21
-
-
33646576245
-
2-Catalyzed Rearrangement of Methyleneyclopropanes
-
- 6307
-
2-Catalyzed Rearrangement of Methyleneyclopropanes J. Am. Chem. Soc. 2006, 128, 6306-6307
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 6306
-
-
Fürstner, A.1
Aïssa, C.2
-
22
-
-
27544467800
-
2-Catalyzed Intramolecular Carboalkoxylation or Carboamination of Alkynes
-
- 15025
-
2- Catalyzed Intramolecular Carboalkoxylation or Carboamination of Alkynes J. Am. Chem. Soc. 2005, 127, 15024-15025
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 15024
-
-
Fürstner, A.1
Davies, P.W.2
-
23
-
-
36749027602
-
Two Manifolds for Metal-Catalyzed Intramolecular Diels-Alder Reactions of Unactivated Alkynes
-
- 8849
-
Fürstner, A.; Stimson, C. C. Two Manifolds for Metal-Catalyzed Intramolecular Diels-Alder Reactions of Unactivated Alkynes Angew. Chem., Int. Ed. 2007, 46, 8845-8849
-
(2007)
Angew. Chem., Int. Ed.
, vol.46
, pp. 8845
-
-
Fürstner, A.1
Stimson, C.C.2
-
24
-
-
4744342870
-
Synthesis of Phenanthrenes and Polycyclic Heteroarenes by Transition-Metal Catalyzed Cycloisomerization Reactions
-
- 4575
-
Mamane, V.; Hannen, P.; Fürstner, A. Synthesis of Phenanthrenes and Polycyclic Heteroarenes by Transition-Metal Catalyzed Cycloisomerization Reactions Chem.-Eur. J. 2004, 10, 4556-4575
-
(2004)
Chem. - Eur. J.
, vol.10
, pp. 4556
-
-
Mamane, V.1
Hannen, P.2
Fürstner, A.3
-
25
-
-
3242691284
-
Platinum- and Gold-Catalyzed Cycloisomerization Reactions of Hydroxylated Enynes
-
- 8655
-
Mamane, V.; Gress, T.; Krause, H.; Fürstner, A. Platinum- and Gold-Catalyzed Cycloisomerization Reactions of Hydroxylated Enynes J. Am. Chem. Soc. 2004, 126, 8654-8655
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 8654
-
-
Mamane, V.1
Gress, T.2
Krause, H.3
Fürstner, A.4
-
26
-
-
9944255707
-
Carene Terpenoids by Gold-Catalyzed Cycloisomerization Reactions
-
- 2547
-
Fürstner, A.; Hannen, P. Carene Terpenoids by Gold-Catalyzed Cycloisomerization Reactions Chem. Commun. 2004, 2546-2547
-
(2004)
Chem. Commun.
, pp. 2546
-
-
Fürstner, A.1
Hannen, P.2
-
27
-
-
33746216354
-
Synthesis of (-)-Cubebol by Face-Selective Platinum-, Gold- or Copper-Catalyzed Cycloisomerization: Evidence for Chirality Transfer
-
For a closely related approach, see - 2904
-
For a closely related approach, see: Fehr, C.; Galindo, J. Synthesis of (-)-Cubebol by Face-Selective Platinum-, Gold- or Copper-Catalyzed Cycloisomerization: Evidence for Chirality Transfer Angew. Chem., Int. Ed. 2006, 45, 2901-2904
-
(2006)
Angew. Chem., Int. Ed.
, vol.45
, pp. 2901
-
-
Fehr, C.1
Galindo, J.2
-
31
-
-
33645688330
-
Platinum- and Gold-Catalyzed Rearrangement Reactions of Propargyl Acetates: Total Syntheses of (-)-α-Cubebene, (-)-Cubebol, Sesquicarene and Related Terpenes
-
- 3019
-
Fürstner, A.; Hannen, P. Platinum- and Gold-Catalyzed Rearrangement Reactions of Propargyl Acetates: Total Syntheses of (-)-α-Cubebene, (-)-Cubebol, Sesquicarene and Related Terpenes Chem.-Eur. J. 2006, 12, 3006-3019
-
(2006)
Chem. - Eur. J.
, vol.12
, pp. 3006
-
-
Fürstner, A.1
Hannen, P.2
-
32
-
-
55049084033
-
A Gold-Catalyzed Entry into the Sesquisabinene and Sesquithujene Families of Terpenoids and a Formal Total Synthesis of Cedrene and Cedrol
-
- 9191
-
Fürstner, A.; Schlecker, A. A Gold-Catalyzed Entry into the Sesquisabinene and Sesquithujene Families of Terpenoids and a Formal Total Synthesis of Cedrene and Cedrol Chem.-Eur. J. 2008, 14, 9181-9191
-
(2008)
Chem. - Eur. J.
, vol.14
, pp. 9181
-
-
Fürstner, A.1
Schlecker, A.2
-
33
-
-
33749327279
-
Total Syntheses of the Tylophora Alkaloids Cryptopleurine, (-)-Antofine, (-)-Tylophorine, and (-)-Ficuseptine C
-
- 7410
-
Fürstner, A.; Kennedy, J. W. J. Total Syntheses of the Tylophora Alkaloids Cryptopleurine, (-)-Antofine, (-)-Tylophorine, and (-)-Ficuseptine C Chem.-Eur. J. 2006, 12, 7398-7410
-
(2006)
Chem. - Eur. J.
, vol.12
, pp. 7398
-
-
Fürstner, A.1
Kennedy, J.W.J.2
-
34
-
-
79955799172
-
Recent Developments in Asymmetric Catalysis in the Presence of Chiral Gold Complexes
-
- 1514
-
Pradal, A.; Toullec, P. Y.; Michelet, V. Recent Developments in Asymmetric Catalysis in the Presence of Chiral Gold Complexes Synthesis 2011, 1501-1514
-
(2011)
Synthesis
, pp. 1501
-
-
Pradal, A.1
Toullec, P.Y.2
Michelet, V.3
-
35
-
-
77949418593
-
Enantioselective Gold Catalysis: Opportunities Provided by Monodentate Phosphoramidite Ligands with an Acyclic TADDOL Backbone
-
- 1953
-
Teller, H.; Flügge, S.; Goddard, R.; Fürstner, A. Enantioselective Gold Catalysis: Opportunities Provided by Monodentate Phosphoramidite Ligands with an Acyclic TADDOL Backbone Angew. Chem., Int. Ed. 2010, 49, 1949-1953
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 1949
-
-
Teller, H.1
Flügge, S.2
Goddard, R.3
Fürstner, A.4
-
36
-
-
84866510167
-
One-Point Binding Ligands for Asymmetric Gold Catalysis: Phosphoramidites with a TADDOL-Related but Acyclic Backbone
-
- 15342
-
Teller, H.; Corbet, M.; Mantilli, L.; Gopakumar, G.; Goddard, R.; Thiel, W.; Fürstner, A. One-Point Binding Ligands for Asymmetric Gold Catalysis: Phosphoramidites with a TADDOL-Related but Acyclic Backbone J. Am. Chem. Soc. 2012, 134, 15331-15342
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 15331
-
-
Teller, H.1
Corbet, M.2
Mantilli, L.3
Gopakumar, G.4
Goddard, R.5
Thiel, W.6
Fürstner, A.7
-
37
-
-
79959662809
-
Concise Synthesis of the Antidepressive Drug Candidate GSK1360707 by a Highly Enantioselective Gold-Catalyzed Enyne Cycloisomerization Reaction
-
- 7767
-
Teller, H.; Fürstner, A. Concise Synthesis of the Antidepressive Drug Candidate GSK1360707 by a Highly Enantioselective Gold-Catalyzed Enyne Cycloisomerization Reaction Chem.-Eur. J. 2011, 17, 7764-7767
-
(2011)
Chem. - Eur. J.
, vol.17
, pp. 7764
-
-
Teller, H.1
Fürstner, A.2
-
38
-
-
78651473264
-
An Enyne Cycloisomerization Approach to the Triple Reuptake Inhibitor GSK1360707F
-
An earlier synthesis had screened a library of chiral ligands in combination with Au(I) but furnished a maximum ee of 59%, see - 715
-
An earlier synthesis had screened a library of chiral ligands in combination with Au(I) but furnished a maximum ee of 59%, see: Deschamps, N. M.; Elitzin, V. I.; Liu, B.; Mitchell, M. B.; Sharp, M. J.; Tabet, E. A. An Enyne Cycloisomerization Approach to the Triple Reuptake Inhibitor GSK1360707F J. Org. Chem. 2011, 76, 712-715
-
(2011)
J. Org. Chem.
, vol.76
, pp. 712
-
-
Deschamps, N.M.1
Elitzin, V.I.2
Liu, B.3
Mitchell, M.B.4
Sharp, M.J.5
Tabet, E.A.6
-
39
-
-
79953705667
-
Phosphoramidite Gold(I)-Catalyzed Diastereo- and Enantioselective Synthesis of 3,4-Substituted Pyrrolidines
-
For another application, see - 5507
-
For another application, see: González, A. Z.; Benitez, D.; Tkatchouk, E.; Goddard, W. A.; Toste, F. D. Phosphoramidite Gold(I)-Catalyzed Diastereo- and Enantioselective Synthesis of 3,4-Substituted Pyrrolidines J. Am. Chem. Soc. 2011, 133, 5500-5507
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 5500
-
-
González, A.Z.1
Benitez, D.2
Tkatchouk, E.3
Goddard, W.A.4
Toste, F.D.5
-
40
-
-
84863709681
-
Total Synthesis of Neurymenolide A Based on a Gold-Catalyzed Synthesis of 4-Hydroxy-2-pyrones
-
- 6933
-
Chaładaj, W.; Corbet, M.; Fürstner, A. Total Synthesis of Neurymenolide A Based on a Gold-Catalyzed Synthesis of 4-Hydroxy-2-pyrones Angew. Chem., Int. Ed. 2012, 51, 6929-6933
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 6929
-
-
Chaładaj, W.1
Corbet, M.2
Fürstner, A.3
-
41
-
-
0041657514
-
Study Towards Bioactive Pyrone Derivatives from the Marine Red Alga Phacelocarpus labillardieri
-
- 6904
-
Song, D.; Blond, G.; Fürstner, A. Study Towards Bioactive Pyrone Derivatives from the Marine Red Alga Phacelocarpus labillardieri Tetrahedron 2003, 59, 6899-6904
-
(2003)
Tetrahedron
, vol.59
, pp. 6899
-
-
Song, D.1
Blond, G.2
Fürstner, A.3
-
42
-
-
69249159098
-
Structure and Bonding in Neutral and Cationic 14-Electron Gold Alkyne π Complexes
-
- 8565
-
Flügge, S.; Anoop, A.; Goddard, R.; Thiel, W.; Fürstner, A. Structure and Bonding in Neutral and Cationic 14-Electron Gold Alkyne π Complexes Chem.-Eur. J. 2009, 15, 8558-8565
-
(2009)
Chem. - Eur. J.
, vol.15
, pp. 8558
-
-
Flügge, S.1
Anoop, A.2
Goddard, R.3
Thiel, W.4
Fürstner, A.5
-
43
-
-
73649120588
-
2-Cooordination to Unsaturated and Aromatic Hydrocarbons: The Key Step in Gold-Catalyzed Organic Transformations
-
- 23
-
2-Cooordination to Unsaturated and Aromatic Hydrocarbons: The Key Step in Gold-Catalyzed Organic Transformations Organometallics 2010, 29, 2-23
-
(2010)
Organometallics
, vol.29
, pp. 2
-
-
Schmidbaur, H.1
Schier, A.2
-
44
-
-
78149425384
-
Elementary Steps in Gold Catalysis: The Significance of gem -Diauration
-
- 8470
-
Seidel, G.; Lehmann, C. W.; Fürstner, A. Elementary Steps in Gold Catalysis: The Significance of gem -Diauration Angew. Chem.; Int. Ed. 2010, 49, 8466-8470
-
(2010)
Angew. Chem.; Int. Ed.
, vol.49
, pp. 8466
-
-
Seidel, G.1
Lehmann, C.W.2
Fürstner, A.3
-
45
-
-
84874639402
-
Alkyne Metathesis on the Rise
-
- 2819
-
Fürstner, A. Alkyne Metathesis on the Rise Angew. Chem., Int. Ed. 2013, 52, 2794-2819
-
(2013)
Angew. Chem., Int. Ed.
, vol.52
, pp. 2794
-
-
Fürstner, A.1
-
46
-
-
77955563276
-
Practical New Silyloxy-Based Alkyne Metathesis Catalysts with Optimized Activity and Selectivity Profiles
-
- 11057
-
Heppekausen, J.; Stade, R.; Goddard, R.; Fürstner, A. Practical New Silyloxy-Based Alkyne Metathesis Catalysts with Optimized Activity and Selectivity Profiles J. Am. Chem. Soc. 2010, 132, 11045-11057
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 11045
-
-
Heppekausen, J.1
Stade, R.2
Goddard, R.3
Fürstner, A.4
-
47
-
-
84864606288
-
Optimized Synthesis, Structural Investigations, Ligand Tuning and Synthetic Evaluation of Silyloxy-Based Alkyne Metathesis Catalysts
-
- 10299
-
Heppekausen, J.; Stade, R.; Kondoh, A.; Seidel, G.; Goddard, R.; Fürstner, A. Optimized Synthesis, Structural Investigations, Ligand Tuning and Synthetic Evaluation of Silyloxy-Based Alkyne Metathesis Catalysts Chem.-Eur. J. 2012, 18, 10281-10299
-
(2012)
Chem. - Eur. J.
, vol.18
, pp. 10281
-
-
Heppekausen, J.1
Stade, R.2
Kondoh, A.3
Seidel, G.4
Goddard, R.5
Fürstner, A.6
-
48
-
-
84875296538
-
Formal Total Synthesis of the Algal Toxin (-)-Polycavernoside A
-
- 4537
-
Brewitz, L.; Llaveria, J.; Yada, A.; Fürstner, A. Formal Total Synthesis of the Algal Toxin (-)-Polycavernoside A Chem.-Eur. J. 2013, 19, 4532-4537
-
(2013)
Chem. - Eur. J.
, vol.19
, pp. 4532
-
-
Brewitz, L.1
Llaveria, J.2
Yada, A.3
Fürstner, A.4
-
49
-
-
0013590923
-
Samarium-catalyzed intramolecular Tishchenko reduction of β-hydroxy ketones. A Stereoselective Approach to the Synthesis of Differentiated anti 1,3-Diol Monoesters
-
- 6449
-
Evans, D. A.; Hoveyda, A. H. Samarium-catalyzed intramolecular Tishchenko reduction of β-hydroxy ketones. A Stereoselective Approach to the Synthesis of Differentiated anti 1,3-Diol Monoesters J. Am. Chem. Soc. 1990, 112, 6447-6449
-
(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 6447
-
-
Evans, D.A.1
Hoveyda, A.H.2
-
50
-
-
77950844810
-
Polycavernoside A: The Prins Macrocyclization Approach
-
- 4565
-
Woo, S. K.; Lee, E. Polycavernoside A: The Prins Macrocyclization Approach J. Am. Chem. Soc. 2010, 132, 4564-4565
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 4564
-
-
Woo, S.K.1
Lee, E.2
-
51
-
-
84985634168
-
Mercury(II) and Palladium(II) Catalyzed [3,3] Sigmatropic Rearrangements
-
- 586
-
Overman, L. E. Mercury(II) and Palladium(II) Catalyzed [3,3] Sigmatropic Rearrangements Angew. Chem., Int. Ed. 1984, 23, 579-586
-
(1984)
Angew. Chem., Int. Ed.
, vol.23
, pp. 579
-
-
Overman, L.E.1
-
52
-
-
79953861207
-
From Total Synthesis to Diverted Total Synthesis: Case Studies in the Amphidinolide Series
-
- 345
-
Fürstner, A. From Total Synthesis to Diverted Total Synthesis: Case Studies in the Amphidinolide Series Isr. J. Chem. 2011, 51, 329-345
-
(2011)
Isr. J. Chem.
, vol.51
, pp. 329
-
-
Fürstner, A.1
-
53
-
-
84880797667
-
Total Synthesis of Amphidinolide F
-
- 9538
-
Valot, G.; Regens, C. S.; O'Malley, D. P.; Godineau, E.; Takikawa, H.; Fürstner, A. Total Synthesis of Amphidinolide F Angew. Chem., Int. Ed. 2013, 52, 9534-9538
-
(2013)
Angew. Chem., Int. Ed.
, vol.52
, pp. 9534
-
-
Valot, G.1
Regens, C.S.2
O'malley, D.P.3
Godineau, E.4
Takikawa, H.5
Fürstner, A.6
-
54
-
-
0035905420
-
Alkyne Metathesis: Development of a Novel Molybdenum-Based Catalyst System and Its Application to the Total Synthesis of Epothilone A and C
-
- 5317
-
Fürstner, A.; Mathes, C.; Lehmann, C. W. Alkyne Metathesis: Development of a Novel Molybdenum-Based Catalyst System and Its Application to the Total Synthesis of Epothilone A and C Chem.-Eur. J. 2001, 7, 5299-5317
-
(2001)
Chem. - Eur. J.
, vol.7
, pp. 5299
-
-
Fürstner, A.1
Mathes, C.2
Lehmann, C.W.3
-
55
-
-
80052432277
-
Second-Generation Total Synthesis of Spirastrellolide F Methyl Ester: The Alkyne Route
-
- 8744
-
Benson, S.; Collin, M.-P.; Arlt, A.; Gabor, B.; Goddard, R.; Fürstner, A. Second-Generation Total Synthesis of Spirastrellolide F Methyl Ester: The Alkyne Route Angew. Chem., Int. Ed. 2011, 50, 8739-8744
-
(2011)
Angew. Chem., Int. Ed.
, vol.50
, pp. 8739
-
-
Benson, S.1
Collin, M.-P.2
Arlt, A.3
Gabor, B.4
Goddard, R.5
Fürstner, A.6
-
56
-
-
72449120372
-
Total Synthesis of Spirastrellolide F Methyl Ester-Part 2: Macrocyclization and Completion of the Synthesis
-
For our earlier synthesis, see - 9950
-
For our earlier synthesis, see: Benson, S.; Collin, M.-P.; O'Neil, G. W.; Ceccon, J.; Fasching, B.; Fenster, M. D. B.; Godbout, C.; Radkowski, K.; Goddard, R.; Fürstner, A. Total Synthesis of Spirastrellolide F Methyl Ester-Part 2: Macrocyclization and Completion of the Synthesis Angew. Chem., Int. Ed. 2009, 48, 9946-9950
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 9946
-
-
Benson, S.1
Collin, M.-P.2
O'neil, G.W.3
Ceccon, J.4
Fasching, B.5
Fenster, M.D.B.6
Godbout, C.7
Radkowski, K.8
Goddard, R.9
Fürstner, A.10
-
57
-
-
84864585876
-
Spirastrellolide B: Construction of the C(26)-C(40) Northern Hemisphere and a Related [5,5,7]-Bis-spiroketal Analogue
-
For a model study toward the northern hemisphere of spirastrellolide via Pt-catalyzed spiroacetal formation, see - 4001
-
For a model study toward the northern hemisphere of spirastrellolide via Pt-catalyzed spiroacetal formation, see: Wang, X.; Paxton, T. J.; Li, N.; Smith, A. B. Spirastrellolide B: Construction of the C(26)-C(40) Northern Hemisphere and a Related [5,5,7]-Bis-spiroketal Analogue Org. Lett. 2012, 14, 3998-4001
-
(2012)
Org. Lett.
, vol.14
, pp. 3998
-
-
Wang, X.1
Paxton, T.J.2
Li, N.3
Smith, A.B.4
-
58
-
-
84884535337
-
Increasing the Structural Span of Alkyne Metathesis
-
- 13058
-
Persich, P.; Llaveria, J.; Lhermet, R.; de Haro, T.; Stade, R.; Kondoh, A.; Fürstner, A. Increasing the Structural Span of Alkyne Metathesis Chem.-Eur. J. 2013, 19, 13047-13058
-
(2013)
Chem. - Eur. J.
, vol.19
, pp. 13047
-
-
Persich, P.1
Llaveria, J.2
Lhermet, R.3
De Haro, T.4
Stade, R.5
Kondoh, A.6
Fürstner, A.7
-
59
-
-
70349823487
-
The Meyer-Schuster Rearrangement for the Synthesis of α,β-Unsaturated Carbonyl Compounds
-
- 4158
-
Engel, D. A.; Dudley, G. B. The Meyer-Schuster Rearrangement for the Synthesis of α,β-Unsaturated Carbonyl Compounds Org. Biomol. Chem. 2009, 7, 4149-4158
-
(2009)
Org. Biomol. Chem.
, vol.7
, pp. 4149
-
-
Engel, D.A.1
Dudley, G.B.2
-
61
-
-
33746066374
-
Total Syntheses of Amphidinolide X and Y
-
- 9204
-
Fürstner, A.; Kattnig, E.; Lepage, O. Total Syntheses of Amphidinolide X and Y J. Am. Chem. Soc. 2006, 128, 9194-9204
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 9194
-
-
Fürstner, A.1
Kattnig, E.2
Lepage, O.3
-
62
-
-
78650702670
-
The Leiodolide B Puzzle
-
- 309
-
Larivée, A.; Unger, J. B.; Thomas, M.; Wirtz, C.; Dubost, C.; Handa, S.; Fürstner, A. The Leiodolide B Puzzle Angew. Chem., Int. Ed. 2011, 50, 304-309
-
(2011)
Angew. Chem., Int. Ed.
, vol.50
, pp. 304
-
-
Larivée, A.1
Unger, J.B.2
Thomas, M.3
Wirtz, C.4
Dubost, C.5
Handa, S.6
Fürstner, A.7
-
63
-
-
33747625671
-
Au(I)-catalyzed Annulation of Enantioenriched Allenes in the Enantioselective Total Synthesis of (-)-Rhazinilam
-
- 10353
-
Liu, Z.; Wasmuth, A. S.; Nelson, S. G. Au(I)-catalyzed Annulation of Enantioenriched Allenes in the Enantioselective Total Synthesis of (-)-Rhazinilam J. Am. Chem. Soc. 2006, 128, 10352-10353
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 10352
-
-
Liu, Z.1
Wasmuth, A.S.2
Nelson, S.G.3
-
64
-
-
84880143408
-
Protecting-Group-Free Total Synthesis of (-)-Rhazinilam and (-)-Rhazinicine Using a Gold-Catalyzed Cascade Cyclization
-
- 7171
-
Sugimoto, K.; Toyoshima, K.; Nonaka, S.; Kotaki, K.; Ueda, H.; Tokuyama, H. Protecting-Group-Free Total Synthesis of (-)-Rhazinilam and (-)-Rhazinicine Using a Gold-Catalyzed Cascade Cyclization Angew. Chem., Int. Ed. 2013, 52, 7168-7171
-
(2013)
Angew. Chem., Int. Ed.
, vol.52
, pp. 7168
-
-
Sugimoto, K.1
Toyoshima, K.2
Nonaka, S.3
Kotaki, K.4
Ueda, H.5
Tokuyama, H.6
-
65
-
-
77952328004
-
Asymmetric, Protecting-Group-Free Total Synthesis of (-)-Englerin A
-
- 3516
-
Zhou, Q.; Chen, X.; Ma, D. Asymmetric, Protecting-Group-Free Total Synthesis of (-)-Englerin A Angew. Chem., Int. Ed. 2010, 49, 3513-3516
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 3513
-
-
Zhou, Q.1
Chen, X.2
Ma, D.3
-
66
-
-
77952397509
-
Enantioselective Synthesis of (-)-Englerins A and B
-
- 3519
-
Molawi, K.; Delpont, N.; Echavarren, A. M. Enantioselective Synthesis of (-)-Englerins A and B Angew. Chem., Int. Ed. 2010, 49, 3517-3519
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 3517
-
-
Molawi, K.1
Delpont, N.2
Echavarren, A.M.3
-
67
-
-
84871979611
-
Total Synthesis and Stereochemical Revision of the Chlorinated Sesquiterpene (±)-Gomerone C
-
- 13069
-
Huwyler, N.; Carreira, E. M. Total Synthesis and Stereochemical Revision of the Chlorinated Sesquiterpene (±)-Gomerone C Angew. Chem., Int. Ed. 2012, 51, 13066-13069
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 13066
-
-
Huwyler, N.1
Carreira, E.M.2
-
68
-
-
77953304460
-
Total Synthesis of (+)-Sieboldine
-
- 7877
-
Canham, S. M.; France, D. J.; Overman, L. E. Total Synthesis of (+)-Sieboldine J. Am. Chem. Soc. 2010, 132, 7876-7877
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 7876
-
-
Canham, S.M.1
France, D.J.2
Overman, L.E.3
-
69
-
-
84864231123
-
A Synthesis of Echinopine B
-
- 7576
-
Michels, T. D.; Dowling, M. S.; Vanderwal, C. D. A Synthesis of Echinopine B Angew. Chem., Int. Ed. 2012, 51, 7572-7576
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 7572
-
-
Michels, T.D.1
Dowling, M.S.2
Vanderwal, C.D.3
-
70
-
-
57049128884
-
Total Synthesis of Bryostatin 16 Using Atom-Economical and Chemoselective Approaches
-
- 488
-
Trost, B. M.; Dong, G. Total Synthesis of Bryostatin 16 Using Atom-Economical and Chemoselective Approaches Nature 2008, 456, 485-488
-
(2008)
Nature
, vol.456
, pp. 485
-
-
Trost, B.M.1
Dong, G.2
-
71
-
-
35048889990
-
Synthesis of Azadirachtin: A Long but Successful Journey
-
- 7632
-
Veitch, G. E.; Beckmann, E.; Burke, B. J.; Boyer, A.; Maslen, S. L.; Ley, S. V. Synthesis of Azadirachtin: A Long but Successful Journey Angew. Chem., Int. Ed. 2007, 46, 7629-7632
-
(2007)
Angew. Chem., Int. Ed.
, vol.46
, pp. 7629
-
-
Veitch, G.E.1
Beckmann, E.2
Burke, B.J.3
Boyer, A.4
Maslen, S.L.5
Ley, S.V.6
-
72
-
-
84865854804
-
Total Synthesis of (-)-Quinocarcin by a Gold(I)-Catalyzed Regioselective Hydroamination
-
- 9172
-
Chiba, H.; Oishi, S.; Fujii, N.; Ohno, H. Total Synthesis of (-)-Quinocarcin by a Gold(I)-Catalyzed Regioselective Hydroamination Angew. Chem., Int. Ed. 2012, 51, 9169-9172
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 9169
-
-
Chiba, H.1
Oishi, S.2
Fujii, N.3
Ohno, H.4
-
73
-
-
84861629455
-
Total Synthesis of (-)-Atrop-Abyssomicin C
-
- 5691
-
Bihelovic, F.; Saicic, R. N. Total Synthesis of (-)-Atrop-Abyssomicin C Angew. Chem., Int. Ed. 2012, 51, 5687-5691
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 5687
-
-
Bihelovic, F.1
Saicic, R.N.2
-
74
-
-
84867553335
-
Studies toward the Unique Pederin Family Member Psymberin: Full Structure Elucidation, Two Alternative Total Syntheses, and Analogues
-
- 17093
-
Feng, Y.; Jiang, X.; De Brabander, J. K. Studies toward the Unique Pederin Family Member Psymberin: Full Structure Elucidation, Two Alternative Total Syntheses, and Analogues J. Am. Chem. Soc. 2012, 134, 17083-17093
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 17083
-
-
Feng, Y.1
Jiang, X.2
De Brabander, J.K.3
-
75
-
-
80053079270
-
Total Syntheses of Drimane-Type Sesquiterpenoids Enabled by a Gold-Catalyzed Tandem Reaction
-
- 14947
-
Shi, H.; Fang, L.; Tan, C.; Shi, L.; Zhang, Q. W.; Li, C.; Luo, T.; Yang, Z. Total Syntheses of Drimane-Type Sesquiterpenoids Enabled by a Gold-Catalyzed Tandem Reaction J. Am. Chem. Soc. 2011, 133, 14944-14947
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 14944
-
-
Shi, H.1
Fang, L.2
Tan, C.3
Shi, L.4
Zhang, Q.W.5
Li, C.6
Luo, T.7
Yang, Z.8
-
76
-
-
84859221039
-
Total Synthesis and Stereochemical Reassignment of (±)-Indoxamycin B
-
- 3477
-
Jeker, O. F.; Carreira, E. M. Total Synthesis and Stereochemical Reassignment of (±)-Indoxamycin B Angew. Chem., Int. Ed. 2012, 51, 3474-3477
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 3474
-
-
Jeker, O.F.1
Carreira, E.M.2
-
77
-
-
84860872900
-
Scalable Total Synthesis of (-)-Berkelic Acid Using a Protecting-Group-Free Strategy
-
Fañanás, F. J.; Mendoza, A.; Arto, T.; Temelli, B.; Rodríguez, F. Scalable Total Synthesis of (-)-Berkelic Acid Using a Protecting-Group-Free Strategy Angew. Chem., Int. Ed. 2012, 51, 4930-4933
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 4930
-
-
Fañanás, F.J.1
Mendoza, A.2
Arto, T.3
Temelli, B.4
Rodríguez, F.5
|